43036-07-3

Basic information

• Product Name: 4-AMINOACETANILIDE HYDROCHLORIDE
• Synonyms: P-AMINOACETANILIDE HCL;N1-(4-AMINOPHENYL)ACETAMIDE HYDROCHLORIDE;N-Acetyl-p-phenylenediamine hydrochloride;4-acetamidoanilinium chloride;N-Acetyl-p-phenylenediamine hydrochloride;P-Aminoacetanilide hydrochloride;P-Acetamidoaniline hydrochloride;P-Acetamidoaniline hydrochloride;P-Aminoacetanilide hydrochloride;4-AcetamidoanilineHCl
• CAS NO: 43036-07-3
• Molecular Formula: C₈H₁₀N₂O*ClH
• Molecular Weight: 186.64
• EINECS: 256-052-1
• Mol File: 43036-07-3.mol
• Article Data: 4

Chemical Properties

• Melting Point: 165 °C
• Boiling Point: 267.7°C at 760 mmHg
• Flash Point: 115.7°C
• Appearance: /
• Vapor Pressure: 0.00802mmHg at 25°C
• BRN: 3703679
• CAS DataBase Reference: 4-AMINOACETANILIDE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-AMINOACETANILIDE HYDROCHLORIDE(43036-07-3)
• EPA Substance Registry System: 4-AMINOACETANILIDE HYDROCHLORIDE(43036-07-3)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• RTECS: AD8225000
• TSCA: Yes
• Hazardous Substances Data: 43036-07-3(Hazardous Substances Data)

Usage

General Description

4-AMINOACETANILIDE HYDROCHLORIDE is a chemical compound that is also known as 4-Aminoacetanilide HCl. It is a hydrochloride salt of 4-aminoacetanilide, which is a white to off-white crystalline powder. 4-AMINOACETANILIDE HYDROCHLORIDE is used in the pharmaceutical industry as an intermediate in the synthesis of various drugs and pharmaceutical products. It is also utilized in the manufacture of dyes and other organic compounds. 4-AMINOACETANILIDE HYDROCHLORIDE is an important chemical in the production of various medications and plays a crucial role in the pharmaceutical and chemical industries.

InChI:InChI=1/C8H10N2O.ClH/c1-6(11)10-8-4-2-7(9)3-5-8;/h2-5H,9H2,1H3,(H,10,11);1H

Upstream product

• 106-50-3 1,4-phenylenediamine 
• 122-80-5 N-acetyl-p-phenylenediamine 

Downstream Products

• 92846-91-8 Mesoxalsaeure-4-acetamidophenylhydrazon 
• 77200-66-9 C₂₄H₂₃N₅O₄ 
• 92650-42-5 Diethylmesoxalat-4-acetamidophenylhydrazon 
• 92024-12-9 Ethylcyanylglyoxylat-4-acetamidophenylhydrazon 

Relevant articles and documents

Cobalt-Catalyzed Deoxygenative Hydroboration of Nitro Compounds and Applications to One-Pot Synthesis of Aldimines and Amides

The commercially available and bench-stable Co(acac)2 ligated with bis[(2-diphenylphosphino)phenyl] ether (dpephos) was employed for selective room temperature hydroboration of nitro compounds with HBPin (TOF up to 4615 h?1), tolerating halide, hydroxy, amino, ether, ester, lactone, amide and heteroaromatic functionalities. These reactions offered a direct access to a variety of N-borylamines RN(H)BPin, which were in situ treated with aldehydes and carboxylic acids to produce a series of aldimines and secondary carboxamides without the need for dehydrating and/or coupling reagents. Combination of these transformations in a sequential one-pot manner allowed for direct and selective synthesis of aldimines and secondary carboxamides from readily available and inexpensive nitro compounds.

Synthesis of some newer formazans and tetrazolium salts and their effect on Ranikhet disease virus and the vaccinia virus

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